A citation-based method for searching scientific literature


List of co-cited articles
84 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Informed consent for clinical treatment.
Daniel E Hall, Allan V Prochazka, Aaron S Fink. CMAJ 2012
106
10

Psychological responses of patients receiving a diagnosis of cancer.
P E Schofield, P N Butow, J F Thompson, M H N Tattersall, L J Beeney, S M Dunn. Ann Oncol 2003
214
10



Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.
Lotte Krabbenborg, L E L M Vissers, J Schieving, T Kleefstra, E J Kamsteeg, J A Veltman, M A Willemsen, S Van der Burg. J Genet Couns 2016
43
7


A discrete choice experiment to assess cancer patients' preferences for when and how to make treatment decisions.
Anne Herrmann, Rob Sanson-Fisher, Alix Hall, Laura Wall, Nicholas Zdenkowski, Amy Waller. Support Care Cancer 2018
11
27

Variation among Consent Forms for Clinical Whole Exome Sequencing.
Sara A Fowler, Carol J Saunders, Mark A Hoffman. J Genet Couns 2018
11
27



Decision aids for people facing health treatment or screening decisions.
Dawn Stacey, France Légaré, Krystina Lewis, Michael J Barry, Carol L Bennett, Karen B Eden, Margaret Holmes-Rovner, Hilary Llewellyn-Thomas, Anne Lyddiatt, Richard Thomson,[...]. Cochrane Database Syst Rev 2017
7

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
5


Readability standards for informed-consent forms as compared with actual readability.
Michael K Paasche-Orlow, Holly A Taylor, Frederick L Brancati. N Engl J Med 2003
382
5


AAGBI: Consent for anaesthesia 2017: Association of Anaesthetists of Great Britain and Ireland.
S M Yentis, A J Hartle, I R Barker, P Barker, D G Bogod, T H Clutton-Brock, A Ruck Keene, S Leifer, A Naughton, E Plunkett. Anaesthesia 2017
55
5

Some limits of informed consent.
O O'Neill. J Med Ethics 2003
217
5

Could Good Care Mean Withholding Information from Patients?
Benjamin D Long, Andrew G Shuman. AMA J Ethics 2016
2
100

The epidemiology and global burden of autism spectrum disorders.
A J Baxter, T S Brugha, H E Erskine, R W Scheurer, T Vos, J G Scott. Psychol Med 2015
354
5

Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay.
Margaret P Adam, April N Justice, Susan Schelley, Andrea Kwan, Louanne Hudgins, Christa L Martin. J Pediatr 2009
22
9

Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
Anna Bremer, MaiBritt Giacobini, Mats Eriksson, Peter Gustavsson, Viviann Nordin, Elisabeth Fernell, Christopher Gillberg, Ann Nordgren, Asa Uppströmer, Britt-Marie Anderlid,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
48
5


Potential Psychosocial Risks of Sequencing Newborns.
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
32
6

Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis.
Lesli A Kiedrowski, Kailey M Owens, Beverly M Yashar, Jane L Schuette. J Genet Couns 2016
31
6

Paternal versus maternal coping styles with child diagnosis of developmental delay.
Yael Barak-Levy, Na'ama Atzaba-Poria. Res Dev Disabil 2013
14
14



Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life.
M Lingen, L Albers, M Borchers, S Haass, J Gärtner, S Schröder, L Goldbeck, R von Kries, K Brockmann, B Zirn. Clin Genet 2016
31
6

"It wasn't a disaster or anything": Parents' experiences of their child's uncertain chromosomal microarray result.
Ella J Wilkins, Alison D Archibald, Margaret A Sahhar, Susan M White. Am J Med Genet A 2016
18
11

Cytogenetic microarrays in Manitoba patients with developmental delay.
A J Dawson, D Riordan, M Tomiuk, D Konkin, T Anderson, P Bocangel, N Lwiwiski, J Saltel-Olson, S Marles, C R Greenberg,[...]. Clin Genet 2009
5
40

Clinical utility of chromosomal microarray analysis.
Jay W Ellison, J Britt Ravnan, Jill A Rosenfeld, S Annie Morton, Nicholas J Neill, Marc S Williams, Jodi Lewis, Beth S Torchia, Cathryn Walker, Ryan N Traylor,[...]. Pediatrics 2012
34
5

Chromosomal microarray testing influences medical management.
Michael E Coulter, David T Miller, David J Harris, Pamela Hawley, Jonathan Picker, Amy E Roberts, Magdi M Sobeih, Mira Irons. Genet Med 2011
77
5

The Diagnostic Yield of Array Comparative Genomic Hybridization Is High Regardless of Severity of Intellectual Disability/Developmental Delay in Children.
Stefano D'Arrigo, Francesco Gavazzi, Enrico Alfei, Orsetta Zuffardi, Cristina Montomoli, Barbara Corso, Erika Buzzi, Francesca L Sciacca, Sara Bulgheroni, Daria Riva,[...]. J Child Neurol 2016
22
9

Prognostic Factors for Poor Cognitive Development in Children Born Very Preterm or With Very Low Birth Weight: A Systematic Review.
Louise Linsell, Reem Malouf, Joan Morris, Jennifer J Kurinczuk, Neil Marlow. JAMA Pediatr 2015
160
5

Social disadvantage and developmental diagnosis in pre-schoolers.
Norma Kayrouz, Susan L Milne, Jenny L McDonald. J Paediatr Child Health 2017
3
66


The role of new genetic technology in investigating autism and developmental delay.
Natasha Shur, Shelly Gunn, Lloyd Feit, Albert K Oh, Yvette Yatchmink, Dianne Abuelo. Med Health R I 2011
3
66


The social licence for research: why care.data ran into trouble.
Pam Carter, Graeme T Laurie, Mary Dixon-Woods. J Med Ethics 2015
126
5

Healthcare professionals' and patients' perspectives on consent to clinical genetic testing: moving towards a more relational approach.
Gabrielle Natalie Samuel, Sandi Dheensa, Bobbie Farsides, Angela Fenwick, Anneke Lucassen. BMC Med Ethics 2017
23
8

Prevalence of and Factors Related to Discordance About Prognosis Between Physicians and Surrogate Decision Makers of Critically Ill Patients.
Douglas B White, Natalie Ernecoff, Praewpannarai Buddadhumaruk, Seoyeon Hong, Lisa Weissfeld, J Randall Curtis, John M Luce, Bernard Lo. JAMA 2016
103
5

The accuracy of surrogate decision makers: a systematic review.
David I Shalowitz, Elizabeth Garrett-Mayer, David Wendler. Arch Intern Med 2006
542
5


Discrete choice experiments to measure consumer preferences for health and healthcare.
Rosalie Viney, Emily Lancsar, Jordan Louviere. Expert Rev Pharmacoecon Outcomes Res 2002
102
5


Barriers to goals of care discussions with seriously ill hospitalized patients and their families: a multicenter survey of clinicians.
John J You, James Downar, Robert A Fowler, François Lamontagne, Irene W Y Ma, Dev Jayaraman, Jennifer Kryworuchko, Patricia H Strachan, Roy Ilan, Aman P Nijjar,[...]. JAMA Intern Med 2015
202
5


Difficult but necessary conversations--the case for advance care planning.
Ian A Scott, Geoffrey K Mitchell, Elizabeth J Reymond, Michael P Daly. Med J Aust 2013
92
5

Breaking bad news: consensus guidelines for medical practitioners.
A Girgis, R W Sanson-Fisher. J Clin Oncol 1995
281
5

Shared decision making--pinnacle of patient-centered care.
Michael J Barry, Susan Edgman-Levitan. N Engl J Med 2012
5


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.